Organocatalytic Enantioselective Construction of Spiroketal Lactones Bearing Axial and Central Chirality via an Asymmetric Domino Reaction-Reference-Cited by-同舟云学术

Organocatalytic Enantioselective Construction of Spiroketal Lactones Bearing Axial and Central Chirality via an Asymmetric Domino Reaction

Published:2022-04-05 Issue:16 Volume:24 Page:2978-2982
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Xu Shiyu¹,Huang Aima¹,Yang Yang¹,Wang Ying²,Zhang Ming¹,Sun Zhihui¹,Zhao Man¹,Wei Yuanlin¹,Li Guofeng²^ORCID,Hong Liang¹^ORCID

Affiliation:

1. Guangdong Key Laboratory of Chiral Molecule and Drug Discovery, School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, Guangdong 510006, China

2. School of Pharmaceutical Sciences, Shenzhen University Health Science Centre, Shenzhen University, Shenzhen, Guangdong 518060, China

Funder

China Postdoctoral Science Foundation

Central University Basic Research Fund of China

National Natural Science Foundation of China

Natural Science Foundation of Guangdong Province

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.2c00845

Reference52 articles.

1. Four New Naphthylisoquinoline Alkaloids from Ancistrocladus tectorius

2. Tumor inhibitors. LXXXX. Steganacin and steganangin, novel antileukemic lignan lactones from Steganotaenia araliacea

3. Die Alkaloide ausMelodinus australis (F. MUELLER) PIERRE (Apocynaceae)

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